Variant: rs1162305984 

    present in Gene: USH2A;LOC102723833
    present in Chromosome: 1
    Position on Chromosome: 216084847
    Alleles of this Variant: A/G

rs1162305984 in USH2A;LOC102723833 gene and RETINITIS PIGMENTOSA 39 (disorder) PMID 28000701 2017 The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands.

PMID 25425308 2014 Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography.

PMID 27318125 2016 A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa.

rs1162305984 in USH2A;LOC102723833 gene and USHER SYNDROME, TYPE IIA PMID 27318125 2016 A combination of two truncating mutations in USH2A causes more severe and progressive hearing impairment in Usher syndrome type IIa.

PMID 25425308 2014 Cone responses in Usher syndrome types 1 and 2 by microvolt electroretinography.

PMID 28000701 2017 The diagnostic yield of whole-exome sequencing targeting a gene panel for hearing impairment in The Netherlands.